Canonical Allele Identifier: CA1737407119

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117666777T= , CM000669.2:g.117666777T=	GRCh38
NC_000007.13:g.117306831T= , CM000669.1:g.117306831T=	GRCh37
NC_000007.12:g.117094067T=	NCBI36
NG_016465.4:g.205994T= , LRG_663:g.205994T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*452-131T=	ENSP00000497673.2:n.*452-131T=
ENST00000647978.2:c.*3957-131T=	ENSP00000497658.1:n.*3957-131T=
ENST00000649781.2:c.4060-131T=	ENSP00000497203.1:n.4060-131T=
ENST00000685018.2:c.*456-131T=	ENSP00000510194.2:n.*456-131T=
ENST00000687278.2:c.*896-825T=	ENSP00000509593.2:n.*896-825T=
ENST00000699585.1:c.*581T=	ENSP00000514456.1:n.*581T=
ENST00000699598.1:c.4243-138T=	ENSP00000514467.1:n.4243-138T=
ENST00000699599.1:c.*456-131T=	ENSP00000514468.1:n.*456-131T=
ENST00000699600.1:c.*904-825T=	ENSP00000514469.1:n.*904-825T=
ENST00000699601.1:c.*2618-131T=	ENSP00000514470.1:n.*2618-131T=
ENST00000699602.1:c.4237-131T=	ENSP00000514471.1:n.4237-131T=
ENST00000699604.1:c.*4067-131T=	ENSP00000514472.1:n.*4067-131T=
ENST00000699605.1:c.3817-131T=	ENSP00000514473.1:n.3817-131T=
ENST00000699606.1:n.3623T=
ENST00000685018.1:c.1107-131T=	ENSP00000510194.1:n.1107-131T=
ENST00000687278.1:c.2030-825T=	ENSP00000509593.1:n.2030-825T=
ENST00000689011.1:c.954T=
ENST00000003084.11:c.4243-131T= MANE Select	ENSP00000003084.6:n.4243-131T=
ENST00000647720.1:c.1693-131T=
ENST00000649781.1:c.4060-131T=	ENSP00000497203.1:n.4060-131T=
ENST00000003084.10:c.4243-131T=	ENSP00000003084.6:n.4243-131T=
ENST00000426809.5:c.4153-131T=	ENSP00000389119.1:n.4153-131T=
ENST00000600166.1:c.368+1213T=
NM_000492.3:c.4243-131T= , LRG_663t1:c.4243-131T=	NP_000483.3:n.4243-131T=
XM_011515751.1:c.4333-131T=	XP_011514053.1:n.4333-131T=
XM_011515752.1:c.*112T=	XP_011514054.1:n.*112T=
XM_011515753.1:c.4000-131T=	XP_011514055.1:n.4000-131T=
XM_011515754.1:c.4000-131T=	XP_011514056.1:n.4000-131T=
NM_000492.4:c.4243-131T= MANE Select	NP_000483.3:n.4243-131T=